Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ammonia | HCID 222 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 4-[(E)-2-Phenylethenyl]benzonitrile | HCID 609608 | — |
| Edukt | Benzimidate | HCID 21972543 | — |
| Edukt | Ethyl-4-styrylbenzimidate hydrochloride | HCID 70566768 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-Styrylbenzamidine hydrochloride | HCID 70565428 | — |
Reaktionsschritte
Hydrogen chloride is bubbled through a mixture of 4-cyanostilbene (13.5 g., 0.065 mole), obtained according to the method of Belgian Pat. No. 641,415 (Chem. Abs. 63: 3092g (1965)), in 35 ml. of dry benzene and 17.5 ml. of absolute ethanol at 0° to 5° C. for a period of 3 hr. The reaction is maintained at 0° to 5° C. for 48 hr. and the solvent and excess hydrogen chloride removed under reduced pressure. The residue stirred with 50 ml. of dry benzene and collected provides 13.0 g. of ethyl-4-styrylbenzimidate hydrochloride. A methanol solution of the benzimidate salt is cooled to 5° to 10° C., saturated with ammonia and heated at a temperature of 100° C. for a period of 3 hr. in an enclosed container. Concentration of the reaction mixture provides 4-styrylbenzamidine hydrochloride.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04096183 |
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| Quelldatensatz | uspto-grants-1978_06 |
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| ORD ID | ord-c553a41648a14f748b5d6a279185da3f |
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| Quellennotiz | uspto-grants-1978_06 |
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